RAS BiologyБиоорганическая химия Russian Journal of Bioorganic Chemistry

  • ISSN (Print) 0132-3423
  • ISSN (Online) 1998-2860

Targeted Nanoliposomes Loaded with IR780 Dye as a Multifunctional Nanoplatform for Photothermal and Photodynamic Cancer Therapy

PII
S19982860S0132342325050132-1
DOI
10.7868/S1998286025050132
Publication type
Article
Status
Published
Authors
Volume/ Edition
Volume 51 / Issue number 5
Pages
882-891
Abstract
During cancer treatment the combined effect of photothermal and photodynamic therapy has unique advantages over each of these methods alone. In this study, a multifunctional targeted nanoplatform for simultaneous combined photothermal and photodynamic therapy under 808 nm infrared laser irradiation was developed. The developed system consists of ~140 nm liposomes specific to the tumor-associated HER2 antigen and loaded with the near-infrared heptamethincyanine dye IR780. The targeting of liposomes to the HER2 is determined by the HER2-specific scaffold protein DARPin_9-29 located on the outer surface of liposomes. It has been established that IR-780, loaded in liposomes, retains photothermal and photodynamic properties: upon irradiation, the temperature of IR780-loaded liposome solution rapidly increases (up to 60°C within 60 s), and the production of reactive oxygen species is also detected. In vitro experiments have shown that HER2-specific liposomes containing IR780 have photoinduced cytotoxicity against HER2-overexpressing cells, causing the death of 50% of the cell population at a concentration of 2.85 μM. The results of the study suggest that HER2-specific liposomes containing IR780 have excellent targeted characteristics, and IR780 can be used as an active substance for simultaneous photothermal and photodynamic therapy.
Keywords
фототермическая терапия фотодинамическая терапия HER2-специфичные липосомы таргетная терапия IR780
Date of publication
01.05.2025
Year of publication
2025
Number of purchasers
0
Views
5

References

  1. 1. Sung H., Ferlay J., Siegel R.L., Laversanne M., Soerjomataram I., Jemal A., Bray F. // CA Cancer J. Clin. 2021. V. 71. P. 209–249. https://doi.org/10.3322/caac.21660
  2. 2. Goto T., Saito H., Sasajima J., Kawamoto T., Fujinaga A., Utsumi T., Yanagawa N., Hiramatsu K., Takamura A., Sato H., Fujibayashi S., Fujiya M. // Front. Oncol. 2020. V. 10. P. 597813. https://doi.org/10.3389/fonc.2020.597813
  3. 3. Nausea and Vomiting Related to Cancer Treatment (PDQ(R)): Health Professional Version // PDQ Cancer Information Summaries. Bethesda (MD), 2002.
  4. 4. Wikramanayake T.C., Haberland N.I., Akhundlu A., Laboy Nieves A., Miteva M. // Curr. Oncol. 2023. V. 30. P. 3609–3626. https://doi.org/10.3390/curroncol30040275
  5. 5. Demoor-Goldschmidt C., de Vathaire F. // Br. J. Radiol. 2019. V. 92. P. 20180390. https://doi.org/10.1259/bjr.20180390
  6. 6. Yoo S.W., Oh G., Ahn J.C., Chung E. // Biomedicines. 2021. V. 9. Р. 113. https://doi.org/10.3390/biomedicines9020113
  7. 7. Han H.S., Choi K.Y. // Biomedicines. 2021. V. 9. Р. 305. https://doi.org/10.3390/biomedicines9030305
  8. 8. Sun J., Zhao H., Xu W., Jiang G.Q. // Front. Chem. 2022. V. 10. P. 1024177. https://doi.org/10.3389/fchem.2022.1024177
  9. 9. Шрамова Е.И., Котляр А.Б., Лебеденко Е.Н., Деев С.М., Прошкина Г.М. // Act. Nat. 2020. V. 12. P. 81–91. https://doi.org/10.32607/actanaturae.11028
  10. 10. Proshkina G.M., Shramova E.I., Serova E.V., Myachev E.A., Mirkasymov A.B., Deyev S.M., Kotlyar A.B. // J. Nanotheranostics. 2025. V. 6. P. 2.
  11. 11. Lin J., Wang S., Huang P., Wang Z., Chen S., Niu G., Li W., He J., Cui D., Lu G., Chen X., Nie Z. // ACS Nano. 2013. V. 7. P. 5320–5329. https://doi.org/10.1021/nn4011686
  12. 12. Zhang M., Murakami T., Ajima K., Tsuchida K., Sandanayaka A.S., Ito O., Iijima S., Yudasaka M. // Proc. Natl. Acad. Sci. USA. 2008. V. 105. P. 14773– 14778. https://doi.org/10.1073/pnas.0801349105
  13. 13. Tian B., Wang C., Zhang S., Feng L., Liu Z. // ACS Nano. 2011. V. 5. P. 7000–7009. https://doi.org/10.1021/nn201560b
  14. 14. Wang K., Zhang Y., Wang J., Yuan A., Sun M., Wu J., Hu Y. // Sci. Rep. 2016. V. 6. P. 27421. https://doi.org/10.1038/srep27421
  15. 15. Gutierrez C., Schiff R. // Arch. Pathol. Lab. Med. 2011. V. 135. P. 55–62. https://doi.org/10.5858/2010-0454-RAR.1
  16. 16. Blumenthal G.M., Scher N.S., Cortazar P., Chattopadhyay S., Tang S., Song P., Liu Q., Ringgold K., Pilaro A.M., Tilley A., King K.E., Graham L., Rellahan B.L., Weinberg W.C., Chi B., Thomas C., Hughes P., Ibrahim A., Justice R., Pazdur R. // Clin. Cancer Res. 2013. V. 19. P. 4911–4916. https://doi.org/10.1158/1078-0432.CCR-13-1212
  17. 17. Steiner D., Forrer P., Pluckthun A. // J. Mol. Biol. 2008. V. 382. P. 1211–1227. https://doi.org/10.1016/j.jmb.2008.07.085
  18. 18. Deyev S., Proshkina G., Baryshnikova O., Ryabova A., Avishai G., Katrivas L., Giannini C., Levi-Kalisman Y., Kotlyar A. // Eur. J. Pharm. Biopharm. 2018. V. 130. P. 296–305. https://doi.org/10.1016/j.ejpb.2018.06.026
QR
Translate

Индексирование

Scopus

Scopus

Scopus

Crossref

Scopus

Higher Attestation Commission

At the Ministry of Education and Science of the Russian Federation

Scopus

Scientific Electronic Library